دورية أكاديمية

A naturally occurring genetic variant of human XRCC2 (R188H) confers increased resistance to cisplatin-induced DNA damage

التفاصيل البيبلوغرافية
العنوان: A naturally occurring genetic variant of human XRCC2 (R188H) confers increased resistance to cisplatin-induced DNA damage
المؤلفون: Danoy, Patrick, Sonoda, Eiichiro, Lathrop, Mark, Takeda, Shunichi, Matsuda, Fumihiko
المساهمون: W. Baumeister
بيانات النشر: Academic Press
سنة النشر: 2007
المجموعة: The University of Queensland: UQ eSpace
مصطلحات موضوعية: DNA repair gene, Homologous recombination, Single nucleotide polymorphism, DT40, Cancer risk, Cisplatin, RAD51, XRCC2, XRCC3, 0601 Biochemistry and Cell Biology, 111201 Cancer Cell Biology, 111203 Cancer Genetics
الوصف: Homologous recombination, a major double strand break repair pathway, plays critical roles in maintaining genome stability. Genetic polymorphisms in HR genes have been implicated in cancer risk. We report a novel assay system for evaluating polymorphisms in human homologous recombination genes using a panel of chicken DT40 repair mutants. We established mutant cell lines complemented with either wild-type or variant cDNAs of three human genes, RAD51, XRCC2, and XRCC3, and assessed their sensitivity to cisplatin and mitomycin C. DT40 mutants complemented with RAD51 coding and 5′UTR variants, and with a XRCC3 coding variant showed equivalent sensitivity as those with wild-type cDNAs. Interestingly, Xrcc2−/− DT40 cells complemented with variant XRCC2 (R188H) were more tolerant to cisplatin than those with wild-type XRCC2. Considering that the XRCC2 (R188H) allele reduces risk to epithelial ovarian cancer, the increased XRCC2 activity with the R188H polymorphism may have clinical benefit in preventing cancer risk.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 0006-291X
1090-2104
الإتاحة: https://doi.org/10.1016/j.bbrc.2006.11.083Test
https://espace.library.uq.edu.au/view/UQ:163791Test
رقم الانضمام: edsbas.BAC03BB1
قاعدة البيانات: BASE